Skip to content

Comparative Efficacy of Lixisenatide and Liraglutide on glucose variability and safety in CGM in Type 2 Diabetes with long-acting insulin

Comparative Efficacy of Lixisenatide and Liraglutide on glucose variability and safety in CGM in Type 2 Diabetes with long-acting insulin - Comparative Efficacy of Lixisenatide and Liraglutide on glucose variability and safety in CGM in Type 2 Diabetes with long-acting insulin

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000020509
Enrollment
32
Registered
2016-01-08
Start date
2015-12-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

type 2 diabetes

Interventions

lixisenatide administration periods:more than 10 days dose:15~20ug the number of times:once a day before breakfast liraglutide administration periods:more than 10 days dose:0.6~0.9mg the num

Sponsors

University of Fukui
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Type 2 diabetic patients being in hospital for the purpose of intensive insulin therapy including long-acting insulin. (Fasting CPR>0.6ng/ml, total bolus insulin <15units/day)

Exclusion criteria

Exclusion criteria: Patients with type 1 diabetes, patients with severe hypoglycemia, patients with severe liver disease, patients with severe renal disease, patients with severe heart disease, patients with history of myocardial infarction within 6 months, patients with severe pancreatic disease, cancer patients, patients with severe diabetic neuropathy, patients with severe diabetic retinopathy, patients with severe ketosis and in a coma, patients with history of digestive diseases, patients with history of gastrectomy, patients with lactose intolerance, heavy drinkers, patients using steroid, pregnant patients

Design outcomes

Primary

MeasureTime frame
MAGE(Mean amplitude of glycemic excursion) of more than 10 days after thrapeutic intervention

Secondary

MeasureTime frame
data in CGM (mean blood glucose, SD, pre-meal plasma glucose in point of care testing, M-value, hypoglycemic index), fasting plasma glucose, 1 hour post prandial glucose, 2 hour post prandial glucose, lipid profile, blood pressure, heart rate, side effect

Countries

Japan

Contacts

Public ContactMichiko Imagawa

University of Fukui Division of Endocrinology and Metabolism, Department of Internal medicine

michikoi@u-fukui.ac.jp0776-61-3111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026